US7414152B2 - N-substituted p-menthane carboxamides - Google Patents

N-substituted p-menthane carboxamides Download PDF

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Publication number
US7414152B2
US7414152B2 US11/437,294 US43729406A US7414152B2 US 7414152 B2 US7414152 B2 US 7414152B2 US 43729406 A US43729406 A US 43729406A US 7414152 B2 US7414152 B2 US 7414152B2
Authority
US
United States
Prior art keywords
menthanecarboxamide
product
menthyl
compound
mouth
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
US11/437,294
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English (en)
Other versions
US20060276667A1 (en
Inventor
Christophe C. Galopin
Pablo Victor Krawec
Jay Patrick Slack
Lori W. Tigani
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Givaudan SA
Original Assignee
Givaudan SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Givaudan SA filed Critical Givaudan SA
Assigned to GIVAUDAN S.A. reassignment GIVAUDAN S.A. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GALOPIN, CHRISTOPHE C., TIGANI, LORI W., KRAWEC, PABLO VICTOR, SLACK, JAY PATRICK
Publication of US20060276667A1 publication Critical patent/US20060276667A1/en
Priority to US12/165,202 priority Critical patent/US20080300314A1/en
Application granted granted Critical
Publication of US7414152B2 publication Critical patent/US7414152B2/en
Priority to US13/222,947 priority patent/USRE44339E1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/58—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton
    • C07C255/60—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton at least one of the singly-bound nitrogen atoms being acylated
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42—Amides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/57—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C233/60—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/57—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C233/61—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
    • C07C255/32—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
    • C07C255/42—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being further bound to other hetero atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
    • C07C255/32—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
    • C07C255/42—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being further bound to other hetero atoms
    • C07C255/44—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being further bound to other hetero atoms at least one of the singly-bound nitrogen atoms being acylated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/45—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups at least one of the singly-bound nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfonamides
    • C07C311/46—Y being a hydrogen or a carbon atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/24—Thermal properties
    • A61K2800/244—Endothermic; Cooling; Cooling sensation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14—The ring being saturated

Definitions

  • Cooling compounds that is, chemical compounds that impart a cooling sensation to the skin or the mucous membranes of the body, are well known to the art and are widely used in a variety of products such as foodstuffs, tobacco products, beverages, dentifrices, mouthwashes and toiletries.
  • Y and Z are selected independently from the group consisting of H, OH, C1-C4 straight or branched alkyl, and a C1-C4 straight or branched alkoxy;
  • X is (CH 2 ) n —R, where n is 0 or 1 and R is a group with non-bonding electrons, with the provisos that:
  • An embodiment provides for compounds of formula I wherein X is in the 4-position. Additional embodiments provide for compounds of formula I wherein X is in the 4-position and Y and Z are H, OH, Me or OMe. In certain embodiments, Y and Z are selected independently.
  • Useful groups with non-bonding electrons are halogens, OH, OMe, NO 2 , CN, Ac, SO 2 NH 2 , CHO, CO 2 H and C 1 -C 4 alkyl carboxylates such as CO 2 Et.
  • Other C 1 -C 4 alkyl carboxylates with non-bonding electrons may be useful.
  • the compounds of formula I have 3 chiral centres, giving rise to 8 stereoisomers. All possible stereoisomers are included in the scope of the compounds represented by formula I.
  • the cooling compounds may be prepared by reacting an arylalkylamine derivative with an appropriate acid chloride or carbonyl chloride.
  • the carbonyl chloride can be prepared from 1-menthol ((1R,2S,5R)-2-isopropyl-5-methylcyclohexanol).
  • the cooling compounds are distinguished from similar compounds of the prior art by their surprisingly high cooling effect (up to 10 times higher than that of similar known compounds) and by the longevity of the cooling effect, which adds to their attractiveness in a large variety of products.
  • the subject cooling compounds may be used in products that are applied to the mouth or the skin to give a cooling sensation.
  • applying is meant any form of bringing into contact, for example, oral ingestion or, in the case of tobacco products, inhalation.
  • applying to the skin it may be, for example, by including the compound in a cream or salve, or in a sprayable composition.
  • a method is directed to providing a cooling effect to the mouth or skin by applying thereto a product comprising a compound as hereinabove described.
  • the subject cooling compounds may be used alone or in combination with other cooling compounds known in the art, e.g., menthol, menthone, isopulegol, N-ethyl p-menthanecarboxamide (WS-3), N,2,3-trimethyl-2-isopropylbutanamide (WS-23), menthyl lactate (FrescolatTM ML), menthone glycerine acetal (FrescolatTM MGA), mono-menthyl succinate (PhyscoolTM), mono-menthyl glutarate, O-menthyl glycerine (CoolActTM 10), menthyl-N,N-dimethylsuccinamate or 2-sec-butylcyclohexanone (FreskomentheTM).
  • other cooling compounds known in the art, e.g., menthol, menthone, isopulegol, N-ethyl p-menthanecarboxamide (WS-3), N,2,3-tri

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Birds (AREA)
  • Dermatology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Cosmetics (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Ceramic Products (AREA)
  • Catalysts (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
US11/437,294 2003-11-21 2006-05-19 N-substituted p-menthane carboxamides Ceased US7414152B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US12/165,202 US20080300314A1 (en) 2003-11-21 2008-06-30 Cooling Compounds
US13/222,947 USRE44339E1 (en) 2003-11-21 2011-08-31 N-substituted P-menthane carboxamides

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US52397703P 2003-11-21 2003-11-21
PCT/CH2004/000646 WO2005049553A1 (en) 2003-11-21 2004-10-28 N-substituted p-menthane carbosamided

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/CH2004/000646 Continuation-In-Part WO2005049553A1 (en) 2003-11-21 2004-10-28 N-substituted p-menthane carbosamided

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US12/165,202 Continuation-In-Part US20080300314A1 (en) 2003-11-21 2008-06-30 Cooling Compounds
US13/222,947 Reissue USRE44339E1 (en) 2003-11-21 2011-08-31 N-substituted P-menthane carboxamides

Publications (2)

Publication Number Publication Date
US20060276667A1 US20060276667A1 (en) 2006-12-07
US7414152B2 true US7414152B2 (en) 2008-08-19

Family

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Family Applications (2)

Application Number Title Priority Date Filing Date
US11/437,294 Ceased US7414152B2 (en) 2003-11-21 2006-05-19 N-substituted p-menthane carboxamides
US13/222,947 Expired - Lifetime USRE44339E1 (en) 2003-11-21 2011-08-31 N-substituted P-menthane carboxamides

Family Applications After (1)

Application Number Title Priority Date Filing Date
US13/222,947 Expired - Lifetime USRE44339E1 (en) 2003-11-21 2011-08-31 N-substituted P-menthane carboxamides

Country Status (10)

Country Link
US (2) US7414152B2 (pl)
EP (1) EP1685093B3 (pl)
JP (1) JP4786544B2 (pl)
CN (1) CN100582089C (pl)
AT (1) ATE464283T1 (pl)
BR (1) BRPI0416770B1 (pl)
DE (1) DE602004026619D1 (pl)
ES (1) ES2342466T7 (pl)
PL (1) PL1685093T6 (pl)
WO (1) WO2005049553A1 (pl)

Cited By (30)

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US20080176945A1 (en) * 2005-03-02 2008-07-24 Galopin Christophe C Carboxilic Acid Amides Provoking A Cooling Sensation
US20090163572A1 (en) * 2007-12-19 2009-06-25 Bom David C Cooling Compounds
US20090240223A1 (en) * 2008-02-22 2009-09-24 Raphael Warren Absorbent article comprising lotion composition comprising a cooling agent
US20090306152A1 (en) * 2008-03-20 2009-12-10 Beiersdorf Ag. Cooling cosmetic or dermatological preparations comprising (1r,2s,5r)-2-isopropyl-5-methyl-n-(2-(pyridin-2-yl)ethyl)-cyclohexane carboxamide and/or (1r,2s,5r)-n-(4-cyanomethyl-phenyl)-2-isopropyl-5-methylcyclohexane carboxamide in combination with menthoxypropanediol
US20090311206A1 (en) * 2008-03-20 2009-12-17 Beiersdorf Ag Cooling cosmetic or dermatological preparations comprising (1r,2s,5r)-2-isopropyl-5-methyl-n-(2-(pyridin-2-yl)ethyl)-cyclohexane carboxamide and/or (1r,2s,5r)-n-(4-cyanomethyl-phenyl)-2-isopropyl-5-methylcyclohexane carboxamide for reducing skin reddening
US20100056636A1 (en) * 2006-12-20 2010-03-04 Stefan Michael Furrer N-Substituted-P-Menthane-3-Carboxamide and Uses Thereof
US20100272655A1 (en) * 2009-04-27 2010-10-28 Kathryn Anne Bardsley Menthylcarboxamides and Their Use as Cooling Agents
US20100297038A1 (en) * 2008-01-17 2010-11-25 Givaudan S.A. Benzimidazole Derivatives And Their Use As Cooling Agents
US20110182833A1 (en) * 2007-12-07 2011-07-28 Stefan Michael Furrer Carboxamide Derivatives Having Cooling Properties
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US9023776B2 (en) * 2011-07-26 2015-05-05 Givaudan S.A. Rinse-off compositions comprising lactoyl ethanolamine and a menthanecarboxamide compound
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ES2342466T7 (es) 2012-11-19
ATE464283T1 (de) 2010-04-15
WO2005049553A1 (en) 2005-06-02
DE602004026619D1 (en) 2010-05-27
EP1685093A1 (en) 2006-08-02
PL1685093T3 (pl) 2010-10-29
CN1878746A (zh) 2006-12-13
BRPI0416770B1 (pt) 2014-05-13
EP1685093B1 (en) 2010-04-14
PL1685093T6 (pl) 2012-10-31

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